Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0512-2021 — Luminesse ML PMMA, 98x20mm, REF: 5336-B1 - Product Usage: used as a milling blank in the fabrication of provisional crowns and bridges. All blanks are solely used by a Trained Dental Technician or on the order of a dental professional.

U.S. FDA — Device Enforcement · United States · 2020-10-09 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0512-2021
Date of alert
2020-10-09
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
Talladium Inc
Product category
device
Product type
Devices
Reported risk: Heat-cured polymethylmethacrylate (PMMA) milling blank product used to make long-term temporary crowns and bridge restorations has incorrect label. label states Part no. 5336-B1 (98x20mm). However, the item inside the box was Part no. 4302-B1 (95x20mm). An incorrect label may result in compatibility issues when setting up the disc with milling machine fixtures due to size variation.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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